Results 131 to 140 of about 1,770 (187)

Impact of long-term elosulfase alfa treatment on respiratory function in patients with Morquio A syndrome. [PDF]

J Inherit Metab Dis, 2016
Hendriksz CJ, Berger KI, Parini R, AlSayed MD, Raiman J, Giugliani R, Mitchell JJ, Burton BK, Guelbert N, Stewart F, Hughes DA, Matousek R, Jurecki E, Decker C, Harmatz PR.   +14 more
europepmc   +1 more source

Clinical and Molecular Characterization of Pakistani Mucopolysaccharidosis Families with <i>SGSH</i> and <i>GALNS</i> Deficiencies. [PDF]

Genes (Basel)
Awan FN, Zulfiqar S, Eiman L, Asif M, Hussain MS, Dahl N, Baig SM, Oda H.   +7 more
europepmc   +1 more source

Therapies of mucopolysaccharidosis IVA (Morquio A syndrome). [PDF]

Expert Opin Orphan Drugs, 2013
Tomatsu S, Alméciga-Díaz CJ, Barbosa H, Montaño AM, Barrera LA, Shimada T, Yasuda E, Mackenzie WG, Mason RW, Suzuki Y, Orii KE, Orii T.   +11 more
europepmc   +1 more source

Impact of elosulfase alfa in patients with morquio A syndrome who have limited ambulation: An open-label, phase 2 study. [PDF]

Am J Med Genet A, 2017
Harmatz PR, Mengel E, Geberhiwot T, Muschol N, Hendriksz CJ, Burton BK, Jameson E, Berger KI, Jester A, Treadwell M, Sisic Z, Decker C.   +11 more
europepmc   +1 more source

Craniovertebral Junction Compression in Patients With Morquio Syndrome: Case Series and Literature Review. [PDF]

Cureus
Rakshit P, Sadayandi Ramesh A, Gopikrishnan R, Mani MK, Sathia Prabhu A.   +4 more
europepmc   +1 more source

A Rare Case of Morquio Syndrome in Palestine: Clinical, Radiological, and Genetic Insights. [PDF]

Cureus
Farah RE, Farah RE, Ayasa IW, Abuisneina S.   +3 more
europepmc   +1 more source

Growth Patterns in MPS IVA and MPS IIIA: A Longitudinal Single-Center Study. [PDF]

J Clin Med
Carmon L, Nassar M, Idan D, Leifman D, Shaki D, Elamour S, Hershkovitz E, Loewenthal N, Haim A, Chacham OS.   +9 more
europepmc   +1 more source

Morquio syndrome - hand

, 2012
openaire   +1 more source

Some of the next articles are maybe not open access.

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Morquio syndrome: Diagnosis in an adult

Joint Bone Spine, 2008
Morquio syndrome or mucopolysaccharidosis (MPS) type IV is a rare autosomal recessive disease in which keratan sulfate builds up in cells. There are two variants, A and B, corresponding to deficiencies of two different enzymes. Type A is usually severe, although considerable clinical variability occurs due to the existence of attenuated phenotypes ...
Catherine, Prat, Olivia, Lemaire, Johan, Bret, Laurent, Zabraniecki, Bernard, Fournié   +4 more
exaly   +3 more sources